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Isosorbide Mononitrate

NDC 42799-958 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA075522
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsISOSORBIDE MONONITRATE (30 mg/1)
Marketing started20170105
Package count2

External sources

Source: openFDA. Public-domain (CC0).